Product Details

SNP ID
rs201398091
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:201491748 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGTCCATTTATAGATGTTTACATG[C/G]TCCTTTCTATCAAGGGACTTCATTT
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
ALS2CR11 PubMed Links

Gene Details

Gene
ALS2CR11
Gene Name
amyotrophic lateral sclerosis 2 chromosome region candidate 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001168216.1 4645 Intron NP_001161688.1
NM_001168217.1 4645 Intron NP_001161689.1
NM_001168221.1 4645 Missense Mutation GAC,GAG D1531E NP_001161693.1
NM_152525.5 4645 Intron NP_689738.3
XM_006712331.3 4645 Intron XP_006712394.1
XM_006712332.3 4645 Intron XP_006712395.1
XM_006712333.3 4645 Intron XP_006712396.1
XM_006712334.3 4645 Intron XP_006712397.1
XM_006712335.3 4645 Intron XP_006712398.1
XM_006712336.3 4645 Intron XP_006712399.1
XM_011510736.2 4645 Intron XP_011509038.1

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